Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA.
Annu Rev Biomed Eng. 2012;14:17-46. doi: 10.1146/annurev-bioeng-071811-150054. Epub 2012 Apr 18.
Mucosal surfaces are a major portal of entry for many human pathogens that are the cause of infectious diseases worldwide. Vaccines capable of eliciting mucosal immune responses can fortify defenses at mucosal front lines and protect against infection. However, most licensed vaccines are administered parenterally and fail to elicit protective mucosal immunity. Immunization by mucosal routes may be more effective at inducing protective immunity against mucosal pathogens at their sites of entry. Recent advances in our understanding of mucosal immunity and identification of correlates of protective immunity against specific mucosal pathogens have renewed interest in the development of mucosal vaccines. Efforts have focused on efficient delivery of vaccine antigens to mucosal sites that facilitate uptake by local antigen-presenting cells to generate protective mucosal immune responses. Discovery of safe and effective mucosal adjuvants are also being sought to enhance the magnitude and quality of the protective immune response.
黏膜表面是许多人类病原体的主要入口,这些病原体是导致全球传染病的原因。能够引发黏膜免疫反应的疫苗可以加强黏膜前沿的防御,防止感染。然而,大多数许可的疫苗是通过注射给药的,无法引发保护性的黏膜免疫。通过黏膜途径免疫接种可能更有效地在黏膜病原体进入的部位诱导针对它们的保护性免疫。我们对黏膜免疫的理解的最新进展以及对针对特定黏膜病原体的保护性免疫相关性的鉴定,重新激发了对黏膜疫苗开发的兴趣。研究重点是将疫苗抗原有效递送至黏膜部位,促进局部抗原呈递细胞摄取,从而产生保护性黏膜免疫反应。还在努力寻找安全有效的黏膜佐剂,以增强保护性免疫反应的幅度和质量。
Annu Rev Biomed Eng. 2012-4-18
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